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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

K10008 — Class I MDR by Improving Mobility…

MD Atlas
Improving Mobility Development SL

EUDAMED last updated this device on Apr 1, 2025

K10008

436584K10000ADD

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Improving Mobility Development SL
UDI-DI code: 08436584361145
Reference / catalog number: K10008

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Manufacturer information

Organization name: Improving Mobility Development SL
SRN: ES-MF-000010985
Manufacturer status: Active

Related devices

K10010436584K10000BDFOn the market K10009436584K10000BDFOn the market K30036436584K30000AE7On the market K40050436584K40000AELOn the market K40014436584K40000AELOn the market

Market distribution

Primary placement in Spain; available across 1 country total.

Placed on the market in Spain; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 08436584361145
Basic UDI-DI: 436584K10000ADD
Reference / catalog number: K10008
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Muleta de codo está fabricada en fibra de carbono. Dispone de un sistema de plegado con banda elástica que permite un montaje rápido y seguro (longitud de la muleta plegada: 55 cm). La empuñadura incluye un accesorio reflectante, la contera es estrecha de caucho 100% natural, y ofrece 10 regulaciones de altura para usuarios de 97 a 120 cm. Soporta un peso máximo de usuario de 136 kg
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y12030601ELBOW CRUTCHES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.